"Ambry Genetics"[submitter] AND "FAT2"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2595077	NM_001447.3(FAT2):c.13042A>G (p.Met4348Val)	FAT2, SLC36A1 (M4348V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302136	NM_001447.3(FAT2):c.13003G>A (p.Asp4335Asn)	FAT2, SLC36A1 (D4335N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093104	NM_001447.3(FAT2):c.12959C>T (p.Ala4320Val)	FAT2, SLC36A1 (A4320V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260185	NM_001447.3(FAT2):c.12958G>A (p.Ala4320Thr)	FAT2, SLC36A1 (A4320T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2610076	NM_001447.3(FAT2):c.12941T>A (p.Val4314Glu)	FAT2, SLC36A1 (V4314E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2022917	NM_001447.3(FAT2):c.12913G>A (p.Ala4305Thr)	SLC36A1, FAT2 (A4305T)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2170951	NM_001447.3(FAT2):c.12902G>A (p.Arg4301His)	FAT2, SLC36A1 (R4301H)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1914014	NM_001447.3(FAT2):c.12881G>T (p.Gly4294Val)	FAT2, SLC36A1 (G4294V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2464052	NM_001447.3(FAT2):c.12866G>A (p.Cys4289Tyr)	FAT2, SLC36A1 (C4289Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550060	NM_001447.3(FAT2):c.12854G>T (p.Gly4285Val)	FAT2, SLC36A1 (G4285V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277809	NM_001447.3(FAT2):c.12845G>A (p.Arg4282Gln)	FAT2, SLC36A1 (R4282Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340806	NM_001447.3(FAT2):c.12790G>A (p.Val4264Ile)	FAT2, SLC36A1 (V4264I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093103	NM_001447.3(FAT2):c.12785G>A (p.Arg4262His)	FAT2, SLC36A1 (R4262H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2241812	NM_001447.3(FAT2):c.12779G>A (p.Arg4260Gln)	FAT2, SLC36A1 (R4260Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2199688	NM_001447.3(FAT2):c.12764G>A (p.Arg4255Gln)	FAT2, SLC36A1 (R4255Q)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1984157	NM_001447.3(FAT2):c.12682T>C (p.Phe4228Leu)	FAT2, SLC36A1 (F4228L)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2262919	NM_001447.3(FAT2):c.12647T>C (p.Met4216Thr)	FAT2, SLC36A1 (M4216T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404813	NM_001447.3(FAT2):c.12626G>A (p.Arg4209His)	FAT2, SLC36A1 (R4209H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093102	NM_001447.3(FAT2):c.12611C>T (p.Pro4204Leu)	FAT2, SLC36A1 (P4204L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477887	NM_001447.3(FAT2):c.12466C>T (p.His4156Tyr)	FAT2, SLC36A1 (H4156Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1898871	NM_001447.3(FAT2):c.12460C>A (p.Pro4154Thr)	FAT2, SLC36A1 (P4154T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2712768	NM_001447.3(FAT2):c.12440G>C (p.Arg4147Thr)	FAT2, SLC36A1 (R4147T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2237687	NM_001447.3(FAT2):c.12356C>T (p.Pro4119Leu)	FAT2, SLC36A1 (P4119L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472149	NM_001447.3(FAT2):c.12349C>A (p.Pro4117Thr)	FAT2, SLC36A1 (P4117T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270791	NM_001447.3(FAT2):c.12339C>A (p.Asn4113Lys)	FAT2, SLC36A1 (N4113K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383276	NM_001447.3(FAT2):c.12323C>T (p.Ala4108Val)	FAT2, SLC36A1 (A4108V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2066067	NM_001447.3(FAT2):c.12320G>A (p.Ser4107Asn)	FAT2, SLC36A1 (S4107N)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2555143	NM_001447.3(FAT2):c.12314C>A (p.Pro4105Gln)	FAT2, SLC36A1 (P4105Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093101	NM_001447.3(FAT2):c.12304G>A (p.Glu4102Lys)	FAT2, SLC36A1 (E4102K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275371	NM_001447.3(FAT2):c.12299C>A (p.Ala4100Asp)	FAT2, SLC36A1 (A4100D)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3093100	NM_001447.3(FAT2):c.12283A>G (p.Thr4095Ala)	FAT2, SLC36A1 (T4095A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277445	NM_001447.3(FAT2):c.12170C>T (p.Ala4057Val)	FAT2, SLC36A1 (A4057V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2361564	NM_001447.3(FAT2):c.12163G>A (p.Ala4055Thr)	FAT2, SLC36A1 (A4055T)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2067625	NM_001447.3(FAT2):c.12124G>T (p.Gly4042Trp)	FAT2, SLC36A1 (G4042W)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2144297	NM_001447.3(FAT2):c.12123G>C (p.Arg4041Ser)	FAT2, SLC36A1 (R4041S)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2160521	NM_001447.3(FAT2):c.12074C>T (p.Ala4025Val)	FAT2, SLC36A1 (A4025V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2492426	NM_001447.3(FAT2):c.11962G>C (p.Glu3988Gln)	FAT2, SLC36A1 (E3988Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303692	NM_001447.3(FAT2):c.11921G>A (p.Cys3974Tyr)	FAT2, SLC36A1 (C3974Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2174221	NM_001447.3(FAT2):c.11869C>T (p.Leu3957Phe)	FAT2, SLC36A1 (L3957F)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2197407	NM_001447.3(FAT2):c.11845G>A (p.Asp3949Asn)	FAT2, SLC36A1 (D3949N)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2320291	NM_001447.3(FAT2):c.11810A>G (p.Glu3937Gly)	FAT2, SLC36A1 (E3937G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2421867	NM_001447.3(FAT2):c.11792C>T (p.Thr3931Met)	FAT2, SLC36A1 (T3931M)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 3277805	NM_001447.3(FAT2):c.11758G>A (p.Glu3920Lys)	FAT2, SLC36A1 (E3920K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542771	NM_001447.3(FAT2):c.11591T>C (p.Ile3864Thr)	FAT2, SLC36A1 (I3864T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2966086	NM_001447.3(FAT2):c.11579T>C (p.Met3860Thr)	FAT2, SLC36A1 (M3860T)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2059835	NM_001447.3(FAT2):c.11551G>A (p.Glu3851Lys)	FAT2, SLC36A1 (E3851K)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2518123	NM_001447.3(FAT2):c.11537A>G (p.His3846Arg)	FAT2, SLC36A1 (H3846R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277820	NM_001447.3(FAT2):c.11533C>T (p.Arg3845Cys)	FAT2, SLC36A1 (R3845C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2185845	NM_001447.3(FAT2):c.11452G>A (p.Val3818Ile)	FAT2, SLC36A1 (V3818I)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2064604	NM_001447.3(FAT2):c.11375G>A (p.Arg3792Gln)	FAT2, SLC36A1 (R3792Q)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3093098	NM_001447.3(FAT2):c.11356T>A (p.Tyr3786Asn)	FAT2, SLC36A1 (Y3786N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093097	NM_001447.3(FAT2):c.11331G>T (p.Arg3777Ser)	FAT2, SLC36A1 (R3777S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479579	NM_001447.3(FAT2):c.11264G>C (p.Arg3755Thr)	FAT2, SLC36A1 (R3755T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093096	NM_001447.3(FAT2):c.11249C>T (p.Thr3750Met)	FAT2, SLC36A1 (T3750M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093095	NM_001447.3(FAT2):c.11192C>A (p.Thr3731Asn)	FAT2, SLC36A1 (T3731N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2175329	NM_001447.3(FAT2):c.11171T>C (p.Met3724Thr)	FAT2, SLC36A1 (M3724T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3093094	NM_001447.3(FAT2):c.11156G>A (p.Arg3719Gln)	FAT2, SLC36A1 (R3719Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093093	NM_001447.3(FAT2):c.11032G>A (p.Ala3678Thr)	FAT2, SLC36A1 (A3678T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2063126	NM_001447.3(FAT2):c.10912C>T (p.Leu3638Phe)	FAT2, SLC36A1 (L3638F)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2479663	NM_001447.3(FAT2):c.10855G>C (p.Val3619Leu)	FAT2, SLC36A1 (V3619L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277815	NM_001447.3(FAT2):c.10784G>A (p.Arg3595His)	FAT2, SLC36A1 (R3595H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093091	NM_001447.3(FAT2):c.10775G>A (p.Gly3592Asp)	FAT2, SLC36A1 (G3592D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325860	NM_001447.3(FAT2):c.10745C>T (p.Ala3582Val)	FAT2, SLC36A1 (A3582V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255135	NM_001447.3(FAT2):c.10735T>G (p.Ser3579Ala)	FAT2, SLC36A1 (S3579A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277811	NM_001447.3(FAT2):c.10688C>T (p.Thr3563Met)	FAT2, SLC36A1 (T3563M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 1077283	NM_001447.3(FAT2):c.10666A>G (p.Thr3556Ala)	FAT2, SLC36A1 (T3556A)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3277812	NM_001447.3(FAT2):c.10629T>A (p.Asp3543Glu)	FAT2, SLC36A1 (D3543E)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2137451	NM_001447.3(FAT2):c.10624G>C (p.Glu3542Gln)	FAT2, SLC36A1 (E3542Q)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2069946	NM_001447.3(FAT2):c.10616C>T (p.Thr3539Ile)	FAT2, SLC36A1 (T3539I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2400319	NM_001447.3(FAT2):c.10615A>G (p.Thr3539Ala)	FAT2, SLC36A1 (T3539A)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3093090	NM_001447.3(FAT2):c.10577A>G (p.His3526Arg)	FAT2, LOC132089193 +1 more (H3526R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2073090	NM_001447.3(FAT2):c.10451T>C (p.Val3484Ala)	FAT2, SLC36A1 (V3484A)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2289914	NM_001447.3(FAT2):c.10444T>A (p.Trp3482Arg)	FAT2, SLC36A1 (W3482R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2060447	NM_001447.3(FAT2):c.10413C>A (p.Asn3471Lys)	SLC36A1, FAT2 (N3471K)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1939920	NM_001447.3(FAT2):c.10382C>G (p.Pro3461Arg)	FAT2, SLC36A1 (P3461R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2479812	NM_001447.3(FAT2):c.10366C>T (p.Pro3456Ser)	FAT2, SLC36A1 (P3456S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277818	NM_001447.3(FAT2):c.10322T>C (p.Ile3441Thr)	FAT2, SLC36A1 (I3441T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256498	NM_001447.3(FAT2):c.10275A>T (p.Arg3425Ser)	FAT2, SLC36A1 (R3425S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291382	NM_001447.3(FAT2):c.10271C>T (p.Pro3424Leu)	FAT2, SLC36A1 (P3424L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2985198	NM_001447.3(FAT2):c.10236C>G (p.Ile3412Met)	FAT2, SLC36A1 (I3412M)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2064288	NM_001447.3(FAT2):c.10148C>T (p.Ala3383Val)	FAT2, SLC36A1 (A3383V)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2047682	NM_001447.3(FAT2):c.10126G>T (p.Gly3376Trp)	FAT2, SLC36A1 (G3376W)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2441365	NM_001447.3(FAT2):c.10111A>G (p.Ile3371Val)	FAT2, SLC36A1 (I3371V)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2460172	NM_001447.3(FAT2):c.10027G>T (p.Val3343Leu)	FAT2, SLC36A1 (V3343L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093088	NM_001447.3(FAT2):c.10006G>A (p.Val3336Met)	FAT2, SLC36A1 (V3336M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602479	NM_001447.3(FAT2):c.10000G>A (p.Ala3334Thr)	FAT2, SLC36A1 (A3334T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277808	NM_001447.3(FAT2):c.9971A>T (p.Asp3324Val)	FAT2, SLC36A1 (D3324V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331458	NM_001447.3(FAT2):c.9947A>G (p.Glu3316Gly)	FAT2, SLC36A1 (E3316G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466003	NM_001447.3(FAT2):c.9946G>A (p.Glu3316Lys)	FAT2, SLC36A1 (E3316K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2187345	NM_001447.3(FAT2):c.9910G>A (p.Val3304Met)	FAT2, SLC36A1 (V3304M)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3277806	NM_001447.3(FAT2):c.9884G>A (p.Arg3295Gln)	FAT2, SLC36A1 (R3295Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270378	NM_001447.3(FAT2):c.9880A>T (p.Ser3294Cys)	FAT2, SLC36A1 (S3294C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527013	NM_001447.3(FAT2):c.9844G>C (p.Glu3282Gln)	FAT2, SLC36A1 (E3282Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615304	NM_001447.3(FAT2):c.9827A>G (p.Asn3276Ser)	FAT2, SLC36A1 (N3276S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2173156	NM_001447.3(FAT2):c.9809C>T (p.Thr3270Ile)	FAT2, SLC36A1 (T3270I)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2767624	NM_001447.3(FAT2):c.9805C>T (p.Arg3269Cys)	FAT2, SLC36A1 (R3269C)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2255570	NM_001447.3(FAT2):c.9761G>A (p.Arg3254His)	FAT2, SLC36A1 (R3254H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1984207	NM_001447.3(FAT2):c.9610G>A (p.Val3204Ile)	FAT2, SLC36A1 (V3204I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2882932	NM_001447.3(FAT2):c.9605G>A (p.Gly3202Asp)	FAT2, SLC36A1 (G3202D)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2531970	NM_001447.3(FAT2):c.9589C>A (p.Pro3197Thr)	FAT2, SLC36A1 (P3197T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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